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环境水和植被基质中n-(膦酰基甲基)甘氨酸的液相色谱/电喷雾电离/同位素稀释质谱分析及氨基甲基膦酸的质谱分析

Liquid chromatography/electrospray ionization/isotopic dilution mass spectrometry analysis of n-(phosphonomethyl) glycine and mass spectrometry analysis of aminomethyl phosphonic acid in environmental water and vegetation matrixes.

作者信息

Grey L, Nguyen B, Yang P

机构信息

Ontario Ministry of Environment, Applied Chromatography Section, Ontario, Canada.

出版信息

J AOAC Int. 2001 Nov-Dec;84(6):1770-80.

Abstract

A liquid chromatography/electrospray/mass spectrometry (LC/ES/MS) method was developed for the analysis of glyphosate (n-phosphonomethyl glycine) and its metabolite, aminomethyl phosphonic acid (AMPA) using isotope-labelled glyphosate as a method surrogate. Optimized parameters were achieved to derivatize glyphosate and AMPA using 9-fluorenylmethyl chloroformate (FMOC-Cl) in borate buffer prior to a reversed-phase LC analysis. Method spike recovery data obtained using laboratory and real world sample matrixes indicated an excellent correlation between the recovery of the native and isotope-labelled glyphosate. Hence, the first performance-based, isotope dilution MS method with superior precision, accuracy, and data quality was developed for the analysis of glyphosate. There was, however, no observable correlation between the isotope-labelled glyphosate and AMPA. Thus, the use of this procedure for the accurate analysis of AMPA was not supported. Method detection limits established using standard U.S. Environmental Protection Agency protocol were 0.06 and 0.30 microg/L, respectively, for glyphosate and AMPA in water matrixes and 0.11 and 0.53 microg/g, respectively, in vegetation matrixes. Problems, solutions, and the method performance data related to the analysis of chlorine-treated drinking water samples are discussed. Applying this method to other environmental matrixes, e.g., soil, with minimum modifications is possible, assuring accurate, multimedia studies of glyphosate concentration in the environment and the delivery of useful multimedia information for regulatory applications.

摘要

开发了一种液相色谱/电喷雾/质谱(LC/ES/MS)方法,以同位素标记的草甘膦作为方法替代物,用于分析草甘膦(N-膦酰基甲基甘氨酸)及其代谢物氨甲基膦酸(AMPA)。在反相液相色谱分析之前,优化了参数,以便在硼酸盐缓冲液中使用9-芴基甲基氯甲酸酯(FMOC-Cl)对草甘膦和AMPA进行衍生化。使用实验室和实际样品基质获得的方法加标回收率数据表明,天然草甘膦和同位素标记草甘膦的回收率之间具有良好的相关性。因此,开发了第一种基于性能的、具有卓越精密度、准确度和数据质量的同位素稀释质谱方法,用于分析草甘膦。然而,同位素标记的草甘膦和AMPA之间没有可观察到的相关性。因此,不支持使用该程序对AMPA进行准确分析。按照美国环境保护局标准方案确定的方法检测限,在水基质中草甘膦和AMPA分别为0.06和0.30μg/L,在植被基质中分别为0.11和0.53μg/g。讨论了与分析经氯处理的饮用水样品相关的问题、解决方案和方法性能数据。对该方法进行最少修改后即可应用于其他环境基质,例如土壤,从而确保对环境中草甘膦浓度进行准确的多介质研究,并为监管应用提供有用的多介质信息。

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